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authFullName_s : Emeline Nandrot
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In vitro differentiation of retinal pigment epithelium from adult retinal stem cells

Claudia Aruta , Francesca Giordano , Anna de Marzo , Antonella Comitato , Graça Raposo , et al.
Pigment Cell & melanoma research, 2010, 24 (1), pp.233 - 240. ⟨10.1111/j.1755-148x.2010.00793.x⟩
Journal articles istex hal-03086757v1
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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo , Susanne Kohl , Bart P Leroy , Francis L Munier , Xavier Guillonneau , et al.
American Journal of Human Genetics, 2009, 85, pp.720 - 729. ⟨10.1016/j.ajhg.2009.10.013⟩
Journal articles hal-03086762v1
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Identification of novel genes and altered signaling pathways in the retinal pigment epithelium during the Royal College of Surgeons rat retinal degeneration

Eric M. Dufour , Emeline Nandrot , Dominique Marchant , Loic van den Berghe , Stéphanie Gadin , et al.
Neurobiology of Disease, 2003, pp.166-180
Journal articles hal-03086809v1
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Collectin-11 Is an Important Modulator of Retinal Pigment Epithelial Cell Phagocytosis and Cytokine Production

Xia Dong , Weiju Wu , Liang Ma , Chengfei Liu , Mohajeet B Bhuckory , et al.
Journal of Innate Immunity, 2017, 9, pp.529 - 545. ⟨10.1159/000478042⟩
Journal articles hal-03086718v1

αvβ5 Integrin Receptors at the Apical Surface of the RPE: One Receptor, Two Functions

Emeline Nandrot , Yongen Chang , Silvia Finnemann
Recent Advances in Retinal Degeneration, 613, Springer New York, pp.369-375, 2008, Advances in Experimental Medicine and Biology, ⟨10.1007/978-0-387-74904-4_43⟩
Book sections inserm-03814339v1
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Lack of the antioxidant enzyme methionine sulfoxide reductase A in mice impairs RPE phagocytosis and causes photoreceptor cone dysfunction

Francesca Mazzoni , Ying Dun , Jade A Vargas , Emeline Nandrot , Silvia C Finnemann
Redox Biology, 2021, pp.101918. ⟨10.1016/j.redox.2021.101918⟩
Journal articles hal-03163479v1
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Mutations in Pre-mRNA Processing Factors 3, 8, and 31 Cause Dysfunction of the Retinal Pigment Epithelium

Michael H Farkas , Deborah S Lew , Maria E Sousa , Kinga Bujakowska , Jonathan Chatagnon , et al.
American Journal of Pathology, 2014, 184, pp.2641 - 2652. ⟨10.1016/j.ajpath.2014.06.026⟩
Journal articles hal-03086747v1

Animal Models, in “The Quest to Decipher RPE Phagocytosis”

Emeline Nandrot
Retinal Degenerative Diseases, 801, Springer New York, pp.77-83, 2014, Advances in Experimental Medicine and Biology, ⟨10.1007/978-1-4614-3209-8_10⟩
Book sections inserm-03814345v1
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Otx2- genetically modified retinal pigment epithelial cells rescue photoreceptors after transplantation

Christo Kole , Laurence Klipfel , Ying Yang , Vanessa Ferracane , Frédéric Blond , et al.
Molecular Therapy, 2017, ⟨10.1016/j.ymthe.2017.09.007⟩
Journal articles hal-01611959v1

Altered Rhythm of Photoreceptor Outer Segment Phagocytosis in β5 Integrin Knockout Mice

Emeline Nandrot , Silvia Finnemann
Retinal Degenerative Diseases, 572, Springer US, pp.119-123, 2006, ⟨10.1007/0-387-32442-9_18⟩
Book sections inserm-03814337v1
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CCR2(+) monocytes infiltrate atrophic lesions in age-related macular disease and mediate photoreceptor degeneration in experimental subretinal inflammation in Cx3cr1 deficient mice.

Florian Sennlaub , Constance Auvynet , Bertrand Calippe , Sophie Lavalette , Lucie Poupel , et al.
EMBO Molecular Medicine, 2013, 5 (11), pp.1775-93. ⟨10.1002/emmm.201302692⟩
Journal articles inserm-00912837v1
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Retinal pigment epithelial cells use a MerTK-dependent mechanism to limit the phagocytic particle binding activity of αvβ5 integrin

Emeline Nandrot , Kathryn E Silva , Christina Scelfo , Silvia C Finnemann
Biology of the Cell, 2012, 104, pp.326 - 341. ⟨10.1111/boc.201100076⟩
Journal articles hal-03086754v1
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Dietary antioxidants prevent age-related retinal pigment epithelium actin damage and blindness in mice lacking αvβ5 integrin

Chia-Chia Yu , Emeline Nandrot , Ying Dun , Silvia C Finnemann
Free Radical Biology and Medicine, 2011, 52, pp.660 - 670. ⟨10.1016/j.freeradbiomed.2011.11.021⟩
Journal articles hal-03086755v1
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Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy

Pierre-Henry Gabrielle , Laurence Faivre , Isabelle Audo , Xavier Zanlonghi , Hélène Dollfus , et al.
Scientific Reports, 2021, 11 (1), pp.16412. ⟨10.1038/s41598-021-95743-8⟩
Journal articles hal-03321137v1

A Comprehensive Review of Mutations in the MERTK Proto-Oncogene

Célia Parinot , Emeline Nandrot
Retinal Degenerative Diseases, 854, Springer International Publishing, pp.259-265, 2016, Advances in Experimental Medicine and Biology, ⟨10.1007/978-3-319-17121-0_35⟩
Book sections inserm-03814335v1

On Your Marks… Get Bound… Internalize!

Ah-Lai Law , Emeline Nandrot
Retinal Degenerative Diseases, 723, Springer US, pp.717-722, 2012, Advances in Experimental Medicine and Biology, ⟨10.1007/978-1-4614-0631-0_91⟩
Book sections inserm-03814343v1
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The Signalling Role of the αvβ5-Integrin Can Impact the Efficacy of AAV in Retinal Gene Therapy

Thérèse Cronin , Daniel Chung , Ying Yang , Emeline Nandrot , Jean Bennett
Pharmaceuticals, 2012, 5 (5), pp.447 - 459. ⟨10.3390/ph5050447⟩
Journal articles inserm-02894109v1

Mertk in Daily Retinal Phagocytosis: A History in the Making

Emeline Nandrot , Eric Dufour
Retinal Degenerative Diseases, 664, Springer New York, pp.133-140, 2010, Advances in Experimental Medicine and Biology, ⟨10.1007/978-1-4419-1399-9_16⟩
Book sections inserm-03814340v1
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Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis

Emeline Nandrot , Eric Dufour , Alexandra C Provost , Marie O Péquignot , Sébastien Bonnel , et al.
Neurobiology of Disease, 2000, 7, pp.586 - 599. ⟨10.1006/nbdi.2000.0328⟩
Journal articles istex hal-03086817v1
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Preclinical safety studies of human embryonic stem cell‐derived retinal pigment epithelial cells for the treatment of age‐related macular degeneration

Sandra Petrus-Reurer , Pankaj Kumar , Sara Padrell Sánchez , Monica Aronsson , Helder André , et al.
Stem Cells Translational Medicine, 2020, 9, pp.936 - 953. ⟨10.1002/sctm.19-0396⟩
Journal articles hal-03086697v1

Mertk Activation During RPE Phagocytosis in Vivo Requires αVβ5 Integrin

Silvia Finnemann , Emeline Nandrot
Retinal Degenerative Diseases, Springer US, pp.499-503, 2006, ⟨10.1007/0-387-32442-9_69⟩
Book sections inserm-03814338v1

Human Induced Pluripotent Stem Cells As a Tool to Model a Form of Leber Congenital Amaurosis

Céline Lustremant , Walter Habeler , Alexandra Plancheron , Olivier Goureau , Lydie Grenot , et al.
CELLULAR REPROGRAMMING, 2013, 15 (3), pp.233-246. ⟨10.1089/cell.2012.0076⟩
Journal articles inserm-03814360v1
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Retinal cell type expression specificity of HIV-1-derived gene transfer vectors upon subretinal injection in the adult rat: influence of pseudotyping and promoter.

Alexis-Pierre Bemelmans , Sébastien Bonnel , Leila Houhou , Noëlle Dufour , Emeline Nandrot , et al.
The Journal of Gene Medicine, 2005, 7 (10), pp.1367-1374. ⟨10.1002/jgm.788⟩
Journal articles hal-00187439v1
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Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts

Emeline Nandrot , Christine Slingsby , A Basak , M Cherif-Chefchaouni , B Benazzouz , et al.
Journal of Medical Genetics, 2003
Journal articles hal-03086814v1
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From confluent human iPS cells to self-forming neural retina and retinal pigmented epithelium

Sacha Reichman , Angélique Terray , Amélie Slembrouck , Céline Nanteau , Gaël Orieux , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111, pp.8518 - 8523. ⟨10.1073/pnas.1324212111⟩
Journal articles hal-03086749v1
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Essential role for MFG-E8 as ligand for ␣v␤5 integrin in diurnal retinal phagocytosis

Emeline Nandrot , Monika Anand , Dena Almeida , Kamran Atabai , Dean Sheppard , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2007
Journal articles hal-03086772v1
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Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts

Latifa Hilal , Emeline Nandrot , Mohamed Belmekki , Siham El Bacha , Mohamed Chefchaouni , et al.
Ophthalmic Genetics, 2002
Journal articles hal-03086816v1